Nitrous Oxide

Manufacturer
Helget Gas Products
Effective date
2025-11-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-05-31 22:05:16

Label at a glance#

ProductNitrous Oxide
Active ingredientNITROUS OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE USP
UN1070
CAS: 10024-97-2
DO NOT REMOVE THIS LABEL
DANGER
RX Only
Administration of Nitrous Oxide may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of Nitrous Oxide and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration and with the hazards, contraindications and side effects, and precautions to be taken.
MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY CAUSE DROWSINESS OR DIZZINESS. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY CAUSE FROSTBITE.
Caution: Do not handle until all safety precautions have been read and understood. Keep/store away from combustible materials, clothing. Keep valves and fittings free from oil and grease. Avoid breathing gas. Do not get in eyes, on skin or on clothing. Use and store only outdoors or in a well-ventilated place. In case of fire: Stop leak if safe to do so. Only use equipment rated for cylinder pressure. Use a back flow prevention device in the piping. Use only with equipment cleaned for oxygen service. Open valve slowly. Close valve after each use and when empty. Cylinder temperature should not exceed 52 C (125 F). Use in accordance with Safety Data Sheet for this product.
First Air: IF INHALED, remove to fresh air. If not breathing give artificial respiration. If breathing is difficult, give oxygen. Call a physician. IN CASE of FROSTBITE, obtain immediate medical attention.
HELGET GAS PRODUCTS 4150 S 87TH STREET, OMAHA, NE 68127 866-814-1554 nitrous oxide 1nitrous oxide 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
347046nitrous oxide 99.5 % Gas for InhalationPSN9
347046nitrous oxide 99.5 % Gas for InhalationSCD9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52086-015-01Nitrous Oxide13500 L in 1 CYLINDERGAS135009
52086-015-02Nitrous Oxide4900 L in 1 CYLINDERGAS49009
52086-015-03Nitrous Oxide1150 L in 1 CYLINDERGAS11509
52086-015-04Nitrous Oxide950 L in 1 CYLINDERGAS9509
52086-015-05Nitrous Oxide200 L in 1 CYLINDERGAS2009
52086-015-06Nitrous Oxide2400 L in 1 CYLINDERGAS24009

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52086-01552086-015-01, 52086-015-02, 52086-015-03, 52086-015-04, 52086-015-05, 52086-015-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
NITROUS OXIDEK50XQU1029ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-12-06full-release2026-05-31 21:19:00

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nitrous OxideNITROUS OXIDEHelget Gas Productsc8ea7d9d-d0c3-4ce4-a6e0-3ca0286d97952025-11-12Exact identifier
ndc (package): 52086-015-06
ndc (package): 52086-015-05
ndc (package): 52086-015-04
ndc (package): 52086-015-01
ndc (package): 52086-015-03
ndc (package): 52086-015-02
ndc (product): 52086-015
ndc11 (package): 52086001503
ndc11 (package): 52086001502
ndc11 (package): 52086001501
ndc11 (package): 52086001504
ndc11 (package): 52086001506
ndc11 (package): 52086001505
spl id: 436c1132-5ac7-b396-e063-6394a90adec4
spl set id: c8ea7d9d-d0c3-4ce4-a6e0-3ca0286d9795

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.